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匹伐他汀与新辅助化疗方案联合应用于乳腺癌患者的效果:一项随机对照临床试验。

Effect of concomitant use of pitavastatin with neoadjuvant chemotherapy protocols in breast cancer patients: A randomized controlled clinical trial.

作者信息

Dewidar Samar A, Hamdy Omar, Eltantawy Ahmed, El-Mesery Mohamed, El Gayar Amal M, Soliman Moetaza M

机构信息

Clinical Pharmacy and Pharmacy Practice Department, Faculty of Pharmacy, Mansoura University, Mansoura, Egypt.

Surgical Oncology Department, Oncology Center, Mansoura University, Mansoura University, Mansoura, Egypt.

出版信息

Saudi Pharm J. 2022 Oct;30(10):1486-1496. doi: 10.1016/j.jsps.2022.07.011. Epub 2022 Jul 25.

Abstract

INTRODUCTION

Preclinical studies have demonstrated the possible anticancer effects of statins, but the synergistic effect of concomitant statin use with standard chemotherapy protocols in patients with breast cancer has not yet been investigated.

AIM

The current study aimed to evaluate the efficacy of concomitant pitavastatin use with neoadjuvant chemotherapy protocols in patients with breast cancer.

METHODS

This study was a randomized controlled clinical trial. A total of 70 adult female patients with pathologically-proven invasive breast cancer were randomized to receive or not receive pitavastatin (2 mg) oral tablets once daily concomitantly with standard neoadjuvant chemotherapy protocols for 6 months. The primary outcomes of this study were changes in tumor size and changes to the Ki67 index. In addition, secondary outcomes were changes in cyclin D1 and cleaved caspase-3 serum levels. This study was registered at ClinicalTrials.gov (Identifier: NCT04705909).

RESULTS

Patients in the pitavastatin group showed significantly higher median (IQR) reductions in tumor size [-19.8 (-41.5, 9.5)] compared to those in the control group [-5.0 (-15.5, 0.0), p = 0.0009]. The change in Ki67 from baseline to the end of therapy was similar between the two groups (p = 0.12). By the end of therapy, the cyclin D1 levels in the pitavastatin group were significantly decreased [median (IQR) change of - 10.0 (-20.2, -2.9) from baseline], whereas the control group showed an increase in cyclin D1 levels [14.8 (4.1, 56.4)]. The median (IQR) caspase-3 was elevated in the pitavastatin group 1.6 (0.2, 2.2), and decreased in the control group (-0.2 (-1.1, 0.0), p = 0.0002).Subgroup analysis of the pitavastatin group revealed that patients with positive human epidermal growth receptor 2 (HER2) had higher median (IQR) reductions in Ki67 [-35.0 (-70.0, -12.5)] than those with negative HER2 [2.5 (-15.0, 10.0), p = 0.04]. All patients who achieved a complete pathological response (n = 9) exhibited an HER2-neu positive receptor at baseline.

CONCLUSION

Concomitant use of pitavastatin with standard neoadjuvant chemotherapy protocols may improve neoadjuvant chemotherapy responses in patients with breast cancer.

摘要

引言

临床前研究已证明他汀类药物可能具有抗癌作用,但他汀类药物与标准化疗方案联合使用对乳腺癌患者的协同作用尚未得到研究。

目的

本研究旨在评估匹伐他汀与新辅助化疗方案联合使用对乳腺癌患者的疗效。

方法

本研究为随机对照临床试验。共有70例经病理证实为浸润性乳腺癌的成年女性患者被随机分为两组,一组每天一次口服匹伐他汀(2毫克)片剂,同时接受标准新辅助化疗方案,为期6个月;另一组不接受匹伐他汀治疗。本研究的主要结局指标为肿瘤大小的变化和Ki67指数的变化。此外,次要结局指标为细胞周期蛋白D1和裂解型半胱天冬酶-3血清水平的变化。本研究已在ClinicalTrials.gov注册(标识符:NCT04705909)。

结果

与对照组相比,匹伐他汀组患者的肿瘤大小中位数(四分位间距)显著降低[-19.8(-41.5,9.5)],而对照组为[-5.0(-15.5,0.0),p = 0.0009]。两组从基线到治疗结束时Ki67的变化相似(p = 0.12)。治疗结束时,匹伐他汀组的细胞周期蛋白D1水平显著降低[从基线开始的中位数(四分位间距)变化为-10.(-20.2,-2.9)],而对照组的细胞周期蛋白D1水平升高[14.8(4.1,56.4)]。匹伐他汀组裂解型半胱天冬酶-3的中位数(四分位间距)升高至1.6(0.2,2.2),而对照组降低(-0.2(-1.1,0.0),p = 0.0002)。匹伐他汀组的亚组分析显示,人表皮生长因子受体2(HER2)阳性患者的Ki67中位数(四分位间距)降低幅度[-35.0(-70.0,-12.5)]高于HER2阴性患者[2.5(-15.0,10.0),p = 0.04]。所有达到完全病理缓解的患者(n = 9)在基线时均表现为HER2-neu阳性受体。

结论

匹伐他汀与标准新辅助化疗方案联合使用可能会改善乳腺癌患者的新辅助化疗反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b31/9649354/847d716876e7/ga1.jpg

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